光漂白
类有机物
荧光寿命成像显微镜
体内
荧光
溶酶体
细胞生物学
生物物理学
临床前影像学
材料科学
纳米技术
化学
分辨率(逻辑)
生物
光学
生物化学
物理
生物技术
人工智能
酶
计算机科学
作者
Hongbao Fang,Shankun Yao,Qixin Chen,Chunyan Liu,Yuqi Cai,Shanshan Geng,Yang Bai,Zhiqi Tian,Amanda Zacharias,Takanori Takebe,Yuncong Chen,Zijian Guo,Weijiang He,Jiajie Diao
出处
期刊:ACS Nano
[American Chemical Society]
日期:2019-12-04
卷期号:13 (12): 14426-14436
被引量:68
标识
DOI:10.1021/acsnano.9b08011
摘要
As the cleaners of cells, lysosomes play an important role in circulating organic matter within cells, recovering damaged organelles, and removing waste via endocytosis. Because lysosome dysfunction is associated with various diseases—lysosomal storage diseases, inherited diseases, rheumatoid arthritis, and even shock—it is vital to monitor the movement of lysosomes in cells and in vivo. To that purpose, a method of optical imaging, super-resolution imaging technology (e.g., SIM and STORM), can overcome the limitations of traditional optical imaging and afford a range of possibilities for fluorescence imaging. However, the short wavelength excitation and easy photobleaching of super-resolution fluorescence probes somewhat problematize super-resolution imaging. As described herein, we designed a low-toxicity, photostable, near-infrared small molecule fluorescence probe HD-Br for use in the super-resolution imaging of lysosomes. The interaction of lysosomes and mitochondria was dynamically traced while using the probe's properties to label the lysosomes. Because the probe has the optimal near-infrared excitation and emission wavelengths, liver organoid 3D imaging and Caenorhabditis elegans imaging were also performed. Altogether, our findings indicate valuable approaches and techniques for super-resolution 3D and in vivo imaging.
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